Effects of Korean red ginseng on T-cell repopulation after autologous hematopoietic stem cell transplantation in childhood cancer patients

• Published in: Journal of ginseng research Vol. 48; no. 1; pp. 68 - 76
• Main Authors: Hong, Kyung Taek, Kang, Yeon Jun, Choi, Jung Yoon, Yun, Young Ju, Chang, Il-Moo, Shin, Hee Young, Kang, Hyoung Jin, Lee, Won-Woo
• Format: Journal Article
• Language: English
• Published: Korea (South) Elsevier B.V 2024; 고려인삼학회
• Subjects: Autologous hematopoietic stem cell transplantation; Childhood; Immunosenescence; Korea red ginseng; T cells; 기타의약학; Immunosenescence; Korea red ginseng; T cells; Autologous hematopoietic stem cell transplantation; Childhood; Autologous hematopoietic stem cell; transplantation
• ISSN: 1226-8453; 2093-4947
• DOI: 10.1016/j.jgr.2023.09.001

Although the survival outcomes of childhood cancer patients have improved, childhood cancer survivors suffer from various degrees of immune dysfunction or delayed immune reconstitution. This study aimed to investigate the effect of Korean Red Ginseng (KRG) on T cell recovery in childhood cancer patients who underwent autologous hematopoietic stem cell transplantation (ASCT) from the perspective of inflammatory and senescent phenotypes. This was a single-arm exploratory trial. The KRG group (n = 15) received KRG powder from month 1 to month 12 post-ASCT. We compared the results of the KRG group with those of the control group (n = 23). The proportions of T cell populations, senescent phenotypes, and cytokine production profiles were analyzed at 1, 3, 6, and 12 months post-ASCT using peripheral blood samples. All patients in the KRG group completed the treatment without any safety issues and showed a comparable T cell repopulation pattern to that in the control group. In particular, KRG administration influenced the repopulation of CD4+ T cells via T cell expansion and differentiation into effector memory cell re-expressing CD45RA (EMRA) cells. Although the KRG group showed an increase in the number of CD4+ EMRA cells, the expression of senescent and exhausted markers in these cells decreased, and the capacity for senescence-related cytokine production in the senescent CD28- subset was ameliorated. These findings suggest that KRG promotes the repopulation of CD4+ EMRA T cells and regulates phenotypical and functional senescent changes after ASCT in pediatric patients with cancer. [Display omitted]